Taiwan FDA registration 1fd7cbb7c199d705fe674aa2767630be

“BALTON”Fryderyk Coronary Angioplasty Catheter

TW: “拜登”腓特烈冠狀動脈成形術導管

Taiwan·Risk Class 2·MD·Balton Sp.z o.o.·Registered Apr 17, 2022 – Apr 17, 2027Active

Registration details

Analysis ID: 1fd7cbb7c199d705fe674aa2767630be
License Form: Ministry of Health Medical Device Import No. 035409
Customs Code: DHA05603540904

Company information

Manufacturer: Balton Sp.z o.o.
Manufacturer Country: Poland
Authorized Representative: CATHERINE CONSULTANTS CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E0005 Percutaneous puncture of the coronary ductus
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 17, 2022
Expiry Date: Apr 17, 2027

About this record

Access comprehensive regulatory information for “BALTON”Fryderyk Coronary Angioplasty Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fd7cbb7c199d705fe674aa2767630be and manufactured by Balton Sp.z o.o.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..

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